Analytical Data
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基因名
AQP4
- Application
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别名
Mercurial-insensitive water channel ;MIWCWCH4
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种属
Human
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表达系统
Yeast
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标签
N- His
-
纯度
Greater than 90% as determined by SDS-PAGE.
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蛋白编号
P55087
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表达区间
253-323aa
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分子量
10 kDa
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内毒素
< 1.0 EU per μg protein as determined by the LAL method.
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性状
Freeze-dried powder
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缓冲液
PBS, pH7.4, containing 0.01% SKL, 1mM DTT, 5% Trehalose and Proclin300.
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复溶方法
Reconstitute in ddH2O to a concentration of 0.1-0.5 mg/mL. Do not vortex.
- 个性化定制
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稳定性测试
The thermal stability is described by the loss rate. The loss rate was determined by accelerated thermal degradation test, that is, incubate the protein at 37℃ for 48h, and no obvious degradation and precipitation were observed. The loss rate isless than 8% within the expiration date under appropriate storage condition.
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保存条件 & 期限
Samples are stable for up to twelve months from date of receipt at -20℃ to -80℃. Store it under sterile conditions at -20℃ to -80℃. It is recommended that the protein be aliquoted for optimal storage. Avoid repeated freeze-thaw cycles.
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运输条件
In general, recombinant proteins are supplied as lyophilized powder and shipped at ambient temperature. For bulk packages, the proteins are provided as frozen liquid and shipped with blue ice, unless otherwise requested by the customer.
Quality inspection process
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Protein Description
Aquaporin-4 (AQP4) is a critical water channel protein predominantly expressed in the brain, particularly in astrocytes, where it facilitates water transport across cell membranes. The importance of AQP4 in maintaining brain homeostasis and regulating water balance has drawn significant attention in recent years, with implications for various neurological conditions, including brain edema, multiple sclerosis, and neurodegenerative diseases. Research on recombinant AQP4 proteins aims to elucidate their structure, function, and regulatory mechanisms, which are essential for understanding their role in physiological and pathological processes. Recombinant production of AQP4 allows for detailed biochemical studies, structural analysis through techniques such as X-ray crystallography and cryo-electron microscopy, and the development of specific inhibitors or modulators that can influence AQP4 activity. These investigations not only enhance our comprehension of water transport dynamics in the central nervous system but also pave the way for potential therapeutic strategies targeting AQP4-related disorders. As the field continues to advance, the development of hybrid proteins and novel delivery systems for AQP4 could further enhance our understanding and manipulation of this vital channel, offering promising avenues for research and clinical application.












